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Topics/Oncology/Neoadjuvant Gemcitabine–Cisplatin–Durvalumab for Borderline Resectable Cholangiocarcinoma: Annals of Surgical Oncology | July 2026

Neoadjuvant Gemcitabine–Cisplatin–Durvalumab for Borderline Resectable Cholangiocarcinoma: Annals of Surgical Oncology | July 2026

Clinical knowledge base curated and reviewed by GastroAGI TeamLast updated July 1, 2026

Quick Answer

Introduction: Borderline resectable cholangiocarcinoma (CCA) carries a poor prognosis because many patients cannot undergo curative surgery. Following the approval of gemcitabine–cisplatin–durvalumab (GCD) in advanced biliary tract cancer, this real-world study evaluated its role as neoadjuvant therapy to improve resectability in borderline resectable CCA.


Introduction:

Borderline resectable cholangiocarcinoma (CCA) carries a poor prognosis because many patients cannot undergo curative surgery. Following the approval of gemcitabine–cisplatin–durvalumab (GCD) in advanced biliary tract cancer, this real-world study evaluated its role as neoadjuvant therapy to improve resectability in borderline resectable CCA.

Why was this study needed?

  • Borderline resectable cholangiocarcinoma has low rates of curative resection.
  • Downstaging with neoadjuvant therapy may improve surgical eligibility and long-term survival.
  • The efficacy of gemcitabine–cisplatin–durvalumab in the neoadjuvant setting has not been well established.
  • Real-world data are needed before prospective trials become available.
  • Biomarkers predicting response to neoadjuvant immunotherapy remain undefined.

Results:

  • Neoadjuvant GCD enabled curative surgical resection in 46.2% of patients with anatomically or biologically borderline resectable cholangiocarcinoma, demonstrating meaningful conversion to surgery.
  • All resected patients experienced tumor size reduction, with 83.3% achieving stable disease and 16.7% partial response radiologically, while pathological responses ranged from minimal to complete.
  • Patients who underwent resection had significantly longer overall survival than those who remained unresectable, supporting the value of successful conversion to surgery after neoadjuvant treatment.

Clinical Impact:

This real-world experience suggests that gemcitabine–cisplatin–durvalumab is a feasible and well-tolerated neoadjuvant strategy for carefully selected patients with borderline resectable cholangiocarcinoma. The encouraging conversion-to-resection rate supports further prospective evaluation, while the heterogeneous pathological responses highlight the need for predictive biomarkers to optimize patient selection.

Bottom Line:

Neoadjuvant gemcitabine–cisplatin–durvalumab converted nearly half of borderline resectable cholangiocarcinoma patients to curative surgery and was associated with improved survival in those successfully resected. These findings support further investigation of immunotherapy-based neoadjuvant approaches in biliary tract cancer.

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